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dc.contributor.authorMichelozzi, IM
dc.contributor.authorSufi, J
dc.contributor.authorAdejumo, TA
dc.contributor.authorAmrolia, PJ
dc.contributor.authorTape, CJ
dc.contributor.authorGiustacchini, A
dc.date.accessioned2022-05-27T09:27:03Z
dc.date.available2022-05-27T09:27:03Z
dc.identifier.citationSTAR protocols, 2022, 3 (1), pp. 101174 - ?
dc.identifier.issn2666-1667
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5153
dc.identifier.eissn2666-1667
dc.identifier.doi10.1016/j.xpro.2022.101174
dc.description.abstractHere, we present a comprehensive protocol for the generation and functional characterization of chimeric antigen receptor (CAR) T cells and their products by mass cytometry in a reproducible and scalable manner. We describe the production of CAR T cells from human peripheral blood mononuclear cells. We then detail a three-step staining protocol with metal-labeled antibodies and the subsequent mass cytometry analysis. This protocol allows simultaneous characterization of CAR T cell intracellular signaling, activation, proliferation, cytokine production, and phenotype in a single assay.
dc.formatElectronic-eCollection
dc.format.extent101174 - ?
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectLeukocytes, Mononuclear
dc.subjectT-Lymphocytes
dc.subjectHumans
dc.subjectAntibodies
dc.titleHigh-dimensional functional phenotyping of preclinical human CAR T cells using mass cytometry.
dc.typeJournal Article
dcterms.dateAccepted2022-03-18
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1016/j.xpro.2022.101174
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc-nd/4.0
dc.relation.isPartOfSTAR protocols
pubs.issue1
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Oncogene
pubs.publication-statusPublished
pubs.volume3
pubs.embargo.termsNot known
icr.researchteamOncogene
dc.contributor.icrauthorTape, Christopher


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Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc-nd/4.0/